MMP-25 Metalloprotease Regulates Innate Immune Response through NF-κB Signaling

被引:37
作者
Soria-Valles, Clara [1 ]
Gutierrez-Fernandez, Ana [1 ]
Osorio, Fernando G. [1 ]
Carrero, Dido [1 ]
Ferrando, Adolfo A. [2 ]
Colado, Enrique [3 ]
Soledad Fernandez-Garcia, M. [4 ]
Bonzon-Kulichenko, Elena [5 ]
Vazquez, Jesus [5 ]
Fueyo, Antonio [6 ]
Lopez-Otin, Carlos [1 ]
机构
[1] Univ Oviedo, Fac Med, Dept Bioquim & Biol Mol, Inst Univ Oncol, E-33006 Oviedo, Spain
[2] Columbia Univ, Inst Canc Genet, New York, NY 10032 USA
[3] Hosp Univ Cent Asturias, Serv Hematol, Oviedo 33011, Spain
[4] Hosp Univ Cent Asturias, Serv Anat Patol, Oviedo 33011, Spain
[5] Ctr Nacl Invest Cardiovasc, Lab Prote Cardiovasc, Madrid 28029, Spain
[6] Univ Oviedo, Fac Med, Dept Biol Func, Area Fisiol,Inst Univ Oncol, E-33006 Oviedo, Spain
关键词
MATRIX METALLOPROTEINASES; ACTIVATION; CELLS; INHIBITION; EXPRESSION; MEDIATORS; DEFECTS; MT6-MMP; ENHANCE; BINDING;
D O I
10.4049/jimmunol.1600094
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Matrix metalloproteases (MMP5) regulate innate immunity acting over proinflammatory cytokines, chemokines, and other immune related proteins. MMP-25 (membrane-type 6-MMP) is a membrane-bound enzyme predominantly expressed in leukocytes whose biological function has remained largely unknown. We have generated Mmp25-deficient mice to elucidate the in vivo function of this protease. These mutant mice are viable and fertile and do not show any spontaneous phenotype. However, Mmp25-null mice exhibit a defective innate immune response characterized by low sensitivity to bacterial LPS, hypergammaglobulinemia, and reduced secretion of proinflammatory molecules. Moreover, these immune defects can be tracked to a defective NF-kappa B activation observed in Mmp25-deficient leukocytes. Globally, our findings provide new mechanistic insights into innate immunity through the activity of MMP-25, suggesting that this proteinase could be a potential therapeutic target for immune-related diseases.
引用
收藏
页码:296 / 302
页数:7
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